Gene: CCDC26 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10464870
rs10464870
CCDC26
0.700 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011
dbSNP: rs12544799
rs12544799
CCDC26
0.700 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011
dbSNP: rs16904140
rs16904140
CCDC26
0.700 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011
dbSNP: rs4636162
rs4636162
CCDC26
0.700 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011
dbSNP: rs6985166
rs6985166
CCDC26
0.700 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011
dbSNP: rs9656979
rs9656979
CCDC26
0.700 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011
dbSNP: rs10464870
rs10464870
CCDC26
G 0.700 GeneticVariation GWASDB Genome-wide association study identifies five susceptibility loci for glioma. 19578367

2009
dbSNP: rs16904140
rs16904140
CCDC26
0.700 GeneticVariation GWASDB Genome-wide association study identifies five susceptibility loci for glioma. 19578367

2009
dbSNP: rs6470745
rs6470745
CCDC26
0.720 GeneticVariation BEFREE Taken into consideration the limitations of this study, the present findings suggest a possible participation of rs891835, rs6470745, and rs55705857 as risk factors to develop glioma. 30778791

2019
dbSNP: rs6470745
rs6470745
CCDC26
0.720 GeneticVariation BEFREE Overall, we found three protective alleles for glioma in patients: the allele "G" of rs1801275 in the IL4R gene by allele model (odds ratio [OR], 0.71; 95% confidence interval [CI], 0.50-0.99; P=0.04) and dominant model (OR, 0.67; 95% CI, 0.46-0.99; P=0.04) analysis respectively, the allele "T" of rs17748 in the TREH gene by recessive model (OR, 0.48; 95% CI, 0.23-1.01; P=0.05) analysis, and the allele "G" of rs6470745 in CCDC26 gene by recessive model (OR, 0.48; 95% CI, 0.26-0.89; P=0.02) analysis. 22369735

2012
dbSNP: rs6470745
rs6470745
CCDC26
0.720 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011
dbSNP: rs6470745
rs6470745
CCDC26
0.720 GeneticVariation GWASDB Genome-wide association study identifies five susceptibility loci for glioma. 19578367

2009
dbSNP: rs55705857
rs55705857
CCDC26
0.760 GeneticVariation BEFREE IDH1/2 mutated glioma has been associated with a germline risk variant, the rs55705857 G allele. 30823903

2019
dbSNP: rs55705857
rs55705857
CCDC26
0.760 GeneticVariation BEFREE Of the 6 variants located in 8q24, 2 have strong significant associations with the risk of glioma, including rs4295627 (P = .003, odds ratio [OR] = 1.21), rs55705857 (P = 2.31 × 10, OR = 3.54). 31277128

2019
dbSNP: rs55705857
rs55705857
CCDC26
0.760 GeneticVariation BEFREE Taken into consideration the limitations of this study, the present findings suggest a possible participation of rs891835, rs6470745, and rs55705857 as risk factors to develop glioma. 30778791

2019
dbSNP: rs55705857
rs55705857
CCDC26
G 0.760 GeneticVariation GWASCAT Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21. 29743610

2018
dbSNP: rs55705857
rs55705857
CCDC26
G 0.760 GeneticVariation GWASCAT Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 28346443

2017
dbSNP: rs55705857
rs55705857
CCDC26
0.760 GeneticVariation BEFREE IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation. 27282637

2016
dbSNP: rs55705857
rs55705857
CCDC26
G 0.760 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for glioma. 26424050

2015
dbSNP: rs55705857
rs55705857
CCDC26
0.760 GeneticVariation BEFREE We also adjusted for the recently discovered 8q24 glioma risk locus rs55705857 G allele. 23361564

2013
dbSNP: rs55705857
rs55705857
CCDC26
0.760 GeneticVariation BEFREE Analysis by glioma subtype showed the association with rs55705857 confined to non-glioblastoma multiforme (non-GBM) tumours (P = 1.07 × 10(-67)). 23399484

2013
dbSNP: rs891835
rs891835
CCDC26
0.810 GeneticVariation BEFREE In sub-group analysis, we found that rs891835 and rs6470745 increased the risk of glioma in Europeans and Caucasians. 30778791

2019
dbSNP: rs891835
rs891835
CCDC26
0.810 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011
dbSNP: rs891835
rs891835
CCDC26
G 0.810 GeneticVariation GWASDB Genome-wide association study identifies five susceptibility loci for glioma. 19578367

2009
dbSNP: rs891835
rs891835
CCDC26
G 0.810 GeneticVariation GWASCAT Genome-wide association study identifies five susceptibility loci for glioma. 19578367

2009